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"51660-209-69" National Drug Code (NDC)
Loratadine 1 BLISTER PACK in 1 CARTON (51660-209-69) > 10 TABLET in 1 BLISTER PACK
(Ohm Laboratories Inc.)
NDC Code
51660-209-69
Package Description
1 BLISTER PACK in 1 CARTON (51660-209-69) > 10 TABLET in 1 BLISTER PACK
Product NDC
51660-209
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Loratadine
Non-Proprietary Name
Loratadine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20090623
Marketing Category Name
ANDA
Application Number
ANDA076134
Manufacturer
Ohm Laboratories Inc.
Substance Name
LORATADINE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-209-69